| MADD | Mothers Against Drunk Driving; multiple acyl-CoA dehydrogenase deficiency |
|---|---|
| MCAD | medium chain acyl-CoA dehydrogenase |
| SAG | salicyl acyl glucuronide; sonoangiography; Swiss agammaglobulinemia |
| SCAD | short chain acyl-coenzyme A dehydrogenase |
| VLCAD | very long chain acyl-coenzyme A dehydrogenase |
| acyl-coenzyme A | RCH2COSCoA or RCH2CO~SCoA;condensation product of a carboxylic acid and coenzyme A, and metabolic intermediate of importance, notably in the oxidation and synthesis of fat. Synonym: acyl-coenzyme A. (05 Mar 2000) |
|---|---|
| acyl dihydroxyacetone phosphate oxidoreductase | <enzyme> Forms acyl-sn-glycerol 3-phosphate; uses NADPH Registry number: EC 1.1.1.- (26 Jun 1999) |
| acyl glutamic acid amidohydrolase | <enzyme> Specific for long chain acyl groups such as lauroyl, myristoyl and palmitoyl Registry number: EC 3.5.1.- (26 Jun 1999) |
| acyl-malonyl-ACP synthase | <enzyme> An enzyme condensing malonyl-ACP and acyl-cys-protein to 3-oxoacyl-ACP + cys-protein + CO2, and similar reactions, as steps in fatty acid synthesis; cys-protein is also a part of the fatty acid synthase complex. Synonym: acyl-malonyl-ACP synthase, beta-ketoacyl-ACP synthase. (05 Mar 2000) |
| acyl protein synthetase | <enzyme> Component of the fatty acid reductase complex of luminescent bacteria Registry number: EC 2.3.1.- Synonym: luxe gene product, fatty acyl-protein synthetase (26 Jun 1999) |
| acyl thioester transacylase | <enzyme> Component of the fatty acid synthetase complex; forms acetyl pantetheine from acetyl CoA and pantetheine Registry number: EC 2.3.1.- (26 Jun 1999) |
| beta-hydroxyacyl-(acyl-carrier-protein)dehydrase | <enzyme> In fatty acid synthesis; specific for acyl carrier protein; cannot use acyl CoA; see also faba gene product Registry number: EC 4.2.1.- Synonym: beta-ohacyl-acp dehydrase, beta-hydroxyacyl-acyl carrier protein dehydratase, fabz gene product (26 Jun 1999) |
| branched chain acyl-CoA oxidase | <enzyme> Enzyme from human liver peroxisomes acts on both 2-methyl branched fatty acyl- and bile acid-CoA intermediates, unlike rat liver peroxisomes which have separate enzymes for branched chain fatty acids (pristanoyl-CoA) and bile acid-CoA; involved in beta-oxidation of fatty acids and bil Registry number: EC 1.3.3.- Synonym: 2-methyl-branched chain acyl-CoA oxidase, hbrcacox (26 Jun 1999) |
| malonyl-CoA-acetyl CoA-acyl carrier protein S-acyltransferase | <enzyme> Specific for either malonyl-CoA or acetyl-CoA; a component of fatty acid synthase Registry number: EC 2.8.3.- Synonym: mcoa-acoa acp acyltransferase (26 Jun 1999) |
| medium-chain acyl-CoA dehydrogenase | <enzyme> Deficiency in mitochondrial beta oxidation of fatty acids gives a disorder frequently masquerading as reye syndrome or sudden infant death; leads to buildup of octanoyl carnitine in urine Registry number: EC 1.3.- Synonym: mcaca-dehydrogenase, medium-chain acyl-coenzyme a dehydrogenase, octanoyl-CoA dehydrogenase, mcad enzyme (26 Jun 1999) |
| protein acyl kinase | <enzyme> Transfers gamma-phosphate of ATP to a protein acceptor with formation of an acyl phosphate bond Registry number: EC 2.7.2.- (26 Jun 1999) |
| short-chain acyl-CoA dehydrogenase | See: acyl-CoA dehydrogenase (NADPH+). (05 Mar 2000) |
| N-acyl-D-aspartate amidohydrolase | <enzyme> Specific for d-aspartate; amino acid sequence given in first source Registry number: EC 3.5.1.- Synonym: d-aaase, n-acyl-d-asp amidohydrolase (26 Jun 1999) |
| N-acyl-D-glutamate deacylase | <enzyme> Substrate specificity is for short chain acyl glutamates, including n-formyl-d-glutamate, n-chloroacetyl-d-glutamate and n-acetyl-d-glutamate Registry number: EC 3.5.1.- Synonym: n-acyl-d-glutamate amidohydrolase, d-agase (26 Jun 1999) |
| N-acyl-D-mannosamine dehydrogenase | <enzyme> Catalyses the conversion of n-acetyl-d-mannosamine and nad+ to n-acetyl-d-mannosaminic acid and NADH Registry number: EC 1.1.1.- Synonym: nadm-dehydrogenase, n-acylmannosamine dehydrogenase (26 Jun 1999) |